Pages that link to "Q30482616"
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The following pages link to ENDEAVOUR update: a web resource for gene prioritization in multiple species (Q30482616):
Displaying 50 items.
- Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosis (Q21090977) (← links)
- Predicting the effects of frameshifting indels (Q21184005) (← links)
- In silico gene prioritization by integrating multiple data sources (Q21558505) (← links)
- NEK1 mutations cause short-rib polydactyly syndrome type majewski (Q24324062) (← links)
- Structure and dynamics of molecular networks: a novel paradigm of drug discovery: a comprehensive review (Q27008867) (← links)
- Recent Advances and Emerging Applications in Text and Data Mining for Biomedical Discovery (Q28082443) (← links)
- A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2 Influx (Q28118912) (← links)
- A Novel Prioritization Method in Identifying Recurrent Venous Thromboembolism-Related Genes (Q28551214) (← links)
- Combining heterogenous data for prediction of disease related and pharmacogenes (Q28659646) (← links)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation (Q28685216) (← links)
- Bioinformatics for personal genome interpretation (Q28728835) (← links)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (Q30313778) (← links)
- CLIP-GENE: a web service of the condition specific context-laid integrative analysis for gene prioritization in mouse TF knockout experiments (Q30826367) (← links)
- Identification of novel therapeutics for complex diseases from genome-wide association data. (Q30839676) (← links)
- Linking genes to diseases: it's all in the data. (Q33493193) (← links)
- Gene prioritization and clustering by multi-view text mining (Q33523882) (← links)
- Application of gene network analysis techniques identifies AXIN1/PDIA2 and endoglin haplotypes associated with bicuspid aortic valve (Q33526253) (← links)
- Integration of multiple data sources to prioritize candidate genes using discounted rating system (Q33528193) (← links)
- FAM5C contributes to aggressive periodontitis (Q33552325) (← links)
- Coordinated modular functionality and prognostic potential of a heart failure biomarker-driven interaction network (Q33576324) (← links)
- Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease (Q33590242) (← links)
- A quick guide to large-scale genomic data mining (Q33863385) (← links)
- DDK Promotes Tumor Chemoresistance and Survival via Multiple Pathways. (Q33607399) (← links)
- Decoding the complex genetic causes of heart diseases using systems biology (Q33639681) (← links)
- Clinical Applicability of Whole-Exome Sequencing Exemplified by a Study in Young Adults with the Advanced Cryptogenic Cholestatic Liver Diseases. (Q33775587) (← links)
- CNV-WebStore: online CNV analysis, storage and interpretation (Q33786270) (← links)
- Strategies and issues in the detection of pathway enrichment in genome-wide association studies (Q33832338) (← links)
- Mind the dbGAP: the application of data mining to identify biological mechanisms (Q33888869) (← links)
- PINTA: a web server for network-based gene prioritization from expression data (Q33908012) (← links)
- Information encoded in a network of inflammation proteins predicts clinical outcome after myocardial infarction (Q33960753) (← links)
- Molecular taxonomy of Dunaliella (Chlorophyceae), with a special focus on D. salina: ITS2 sequences revisited with an extensive geographical sampling (Q34240823) (← links)
- Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia (Q34310678) (← links)
- Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes (Q34323019) (← links)
- Prioritization of candidate genes for attention deficit hyperactivity disorder by computational analysis of multiple data sources (Q34330634) (← links)
- GroupRank: rank candidate genes in PPI network by differentially expressed gene groups. (Q34352163) (← links)
- Text mining in cancer gene and pathway prioritization (Q34434966) (← links)
- Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds (Q34506581) (← links)
- Fine mapping and candidate gene search of quantitative trait loci for growth and obesity using mouse intersubspecific subcongenic intercrosses and exome sequencing. (Q34514766) (← links)
- EnRICH: Extraction and Ranking using Integration and Criteria Heuristics (Q34548710) (← links)
- Systems biology elucidates common pathogenic mechanisms between nonalcoholic and alcoholic-fatty liver disease (Q34630137) (← links)
- Transcriptome-based network analysis reveals a spectrum model of human macrophage activation. (Q34659689) (← links)
- Chapter 15: disease gene prioritization (Q34697737) (← links)
- An integrative computational approach for prioritization of genomic variants (Q34704103) (← links)
- Prioritizing disease candidate proteins in cardiomyopathy-specific protein-protein interaction networks based on "guilt by association" analysis (Q34937041) (← links)
- Gentrepid V2.0: a web server for candidate disease gene prediction (Q34942817) (← links)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization (Q34982758) (← links)
- Bioinformatics challenges for personalized medicine (Q35051893) (← links)
- Finding genetic overlaps among diseases based on ranked gene lists. (Q35078429) (← links)
- A computational approach to candidate gene prioritization for X-linked mental retardation using annotation-based binary filtering and motif-based linear discriminatory analysis (Q35124057) (← links)
- Multitask learning of signaling and regulatory networks with application to studying human response to flu (Q35529844) (← links)